128984-81-6Relevant articles and documents
Synthesis of nojirimycin derivatives
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, (2008/06/13)
Nojirimycin δ-lactam and deoxynojirimycin are each synthesized from 5,6-anhydro-3-O-benzyl-1,2-O-isopropylidene-L-idofuranose as a divergent intermediate by a method which comprises formation of the piperidine ring by connection of nitrogen between C-1 and C-5 with inversion of configuration at C-5 to form nojirimycin δ-lactam or between C-2 and C-6 with inversion of configuration at C-2.
SYNTHESIS OF DEOXYNOJIRIMYCIN AND OF NOJIRIMYCIN δ-LACTAM
Fleet, George W.J.,Carpenter, Neil M.,Petursson, Sigthor,Ramsden, Nigel G.
, p. 409 - 412 (2007/10/02)
The syntheses of nojirimycin δ-lactam and of deoxynojirimycin from a divergent ido-furanose intermediate are reported.